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K-Zyme Labs, Inc.

Country not established

Devices
1

What K-Zyme Labs, Inc. makes

K-Zyme Labs, Inc. manufactures the K-Z CONCENTRATE, which is a Class I medical device.

The company is based in the US and its device is listed in the FDA 510(k) registry.

AI-generated from registry data, 3 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • K-Z Concentrate Ref K781011

    Class I
    Active 510(k) 510(k) I

Frequently asked questions

How many devices does K-Zyme Labs, Inc. have in the registry?

The registry currently lists 1 device for K-Zyme Labs, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list K-Zyme Labs, Inc.'s devices?

Among its 1 most recently registered device, K-Zyme Labs, Inc. has devices listed in FDA 510(k) (1 device).

What risk classes do K-Zyme Labs, Inc.'s devices fall under?

Among its 1 most recently registered device, the classes recorded for K-Zyme Labs, Inc.'s devices are Class I. Each device page shows its own class and authorisation.

What are the newest devices from K-Zyme Labs, Inc. in the registry?

The most recently registered devices listed for K-Zyme Labs, Inc. include K-Z CONCENTRATE.

Generated automatically from registry data and not verified by a human reviewer.